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Terminated Phase 2 Interventional Results available

Efficacy and Safety of AQX-1125 in Subjects With Chronic Prostatitis/Chronic Pelvic Pain Syndrome

ClinicalTrials.gov ID: NCT03500159

Public ClinicalTrials.gov record NCT03500159. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:50 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 12-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Trial to Evaluate the Efficacy and Safety of AQX-1125 (200 mg) in Male Subjects With Chronic Prostatitis/Chronic Pelvic Pain Syndrome

Study identification

NCT ID
NCT03500159
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aquinox Pharmaceuticals (Canada) Inc.
Industry
Enrollment
3 participants

Conditions and interventions

Interventions

  • AQX-1125 200 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 17, 2018
Primary completion
Jul 16, 2018
Completion
Jul 16, 2018
Last update posted
Jan 8, 2019

2018

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
22
Facility City State ZIP Site status
Site 1026 Homewood Alabama 35209
Site 1010 Mobile Alabama 36608
Site 1004 Tucson Arizona 85710
Site 1028 Laguna Hills California 92653
Site 1018 Los Alamitos California 90720
Site 1016 Los Angeles California 90048
Site 1020 Los Angeles California 90048
Site 1027 New Port Richey Florida 34653
Site 1013 Coeur d'Alene Idaho 83814
Site 1015 Springfield Illinois 62769
Site 1023 Jeffersonville Indiana 47130
Site 1014 West Des Moines Iowa 50266
Site 1012 Shreveport Louisiana 71106
Site 1002 Royal Oak Michigan 48072
Site 1011 Albuquerque New Mexico 87109
Site 1009 Lake Success New York 11042
Site 1021 Charlotte North Carolina 28207
Site 1008 Raleigh North Carolina 27612
Site 1019 Wilmington North Carolina 28401
Site 1001 Cleveland Ohio 44195
Site 1017 Oklahoma City Oklahoma 73120
Site 1007 Philadelphia Pennsylvania 19140
Site 1022 Dallas Texas 75231

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03500159, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 8, 2019 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03500159 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →